Xue Z, Ziller C, Xue X J
Université Pierre et Marie Curie, Faculté de Médecine Pitié-Salpêtrière, CNRS URA 2115, Paris, France.
Brain Res Dev Brain Res. 1998 Jan 14;105(1):59-66.
The expression of vertebrate homeoproteins has been extensively studied in a variety of normal and cancerous tissues, but little is known on the role of vertebrate homeoproteins in the proliferation and differentiation of cells from these tissues. In the present study, we investigate the relationship between Quox 1 protein (a quail homeodomain containing protein) expression and the proliferation and differentiation of quail dorsal root ganglia (DRG) and neural crest cells. In vivo [3H]TdR labeling experiments demonstrate that the postmitotic sensory neuroblasts appear before the formation of the ganglion, and that more than half of sensory neuroblasts from DRG have already terminated their proliferation in embryos of 2 days of incubation (E2). All DRG neurons have completely ceased to proliferate from E6.5 onwards. By means of immunocytochemistry, we observe that Quox 1 protein is accumulated exclusively in all bipolar neurons in culture of DRG from E9-E11, and in all postmitotic sensory-like neuroblasts during in vitro cell differentiation of the neural crest. The Quox 1 immunoreactive neurons express simultaneously neurofilaments or substance P, and they are never labeled by anti-bromodeoxyuridine. These observations together with the morphology of Quox 1 positive cells, demonstrate that Quox 1 protein is expressed in the postmitotic sensory neurons of DRG. Our previous experiments have shown that between E4 and E6, the accumulation of Quox 1 protein increases in DRG in vivo, but decreases in the central nervous system in which cell proliferation decreases (Xue et al., (1993) Mech. Dev. 43, 149-158). Taken together, our results show that the accumulation of Quox 1 protein in DRG is tightly linked to the increase in the number of postmitotic neurons, whereas in the central nervous system the level of expression of Quox 1 seems concomitant with the extent of cell proliferation.
脊椎动物同源异形蛋白在多种正常组织和癌组织中的表达已得到广泛研究,但对于脊椎动物同源异形蛋白在这些组织细胞增殖和分化中的作用却知之甚少。在本研究中,我们调查了Quox 1蛋白(一种含鹌鹑同源异型结构域的蛋白)表达与鹌鹑背根神经节(DRG)及神经嵴细胞增殖和分化之间的关系。体内[3H]TdR标记实验表明,有丝分裂后感觉神经母细胞在神经节形成之前就已出现,并且来自DRG的一半以上感觉神经母细胞在孵化2天(E2)的胚胎中就已停止增殖。从E6.5开始,所有DRG神经元都完全停止了增殖。通过免疫细胞化学方法,我们观察到Quox 1蛋白仅在E9 - E11期DRG培养物中的所有双极神经元以及神经嵴体外细胞分化过程中的所有有丝分裂后感觉样神经母细胞中积累。Quox 1免疫反应性神经元同时表达神经丝或P物质,并且它们从未被抗溴脱氧尿苷标记。这些观察结果连同Quox 1阳性细胞的形态,表明Quox 1蛋白在DRG的有丝分裂后感觉神经元中表达。我们之前的实验表明,在E4和E6之间,体内DRG中Quox 1蛋白的积累增加,但在细胞增殖减少的中枢神经系统中则减少(薛等人,(1993年)《发育机制》43卷,第149 - 158页)。综合来看,我们的结果表明,DRG中Quox 1蛋白的积累与有丝分裂后神经元数量的增加紧密相关,而在中枢神经系统中,Quox 1的表达水平似乎与细胞增殖程度相关。